YU3696A - Poboljšana sinteza ciklopropilacetilena - Google Patents

Poboljšana sinteza ciklopropilacetilena

Info

Publication number
YU3696A
YU3696A YU3696A YU3696A YU3696A YU 3696 A YU3696 A YU 3696A YU 3696 A YU3696 A YU 3696A YU 3696 A YU3696 A YU 3696A YU 3696 A YU3696 A YU 3696A
Authority
YU
Yugoslavia
Prior art keywords
synthesis
improved
cyclopropylacethylene
cyclopropylacetylene
reverse transcriptase
Prior art date
Application number
YU3696A
Other languages
English (en)
Serbo-Croatian (sh)
Inventor
Andrew Tompson
Edward Corley
Martha Huntington
Original Assignee
Merck & Co. Inc.
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Merck & Co. Inc. filed Critical Merck & Co. Inc.
Publication of YU3696A publication Critical patent/YU3696A/sh

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C13/00Cyclic hydrocarbons containing rings other than, or in addition to, six-membered aromatic rings
    • C07C13/02Monocyclic hydrocarbons or acyclic hydrocarbon derivatives thereof
    • C07C13/04Monocyclic hydrocarbons or acyclic hydrocarbon derivatives thereof with a three-membered ring
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C1/00Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon
    • C07C1/26Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon starting from organic compounds containing only halogen atoms as hetero-atoms
    • C07C1/30Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon starting from organic compounds containing only halogen atoms as hetero-atoms by splitting-off the elements of hydrogen halide from a single molecule
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12Antivirals
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D265/00Heterocyclic compounds containing six-membered rings having one nitrogen atom and one oxygen atom as the only ring hetero atoms
    • C07D265/041,3-Oxazines; Hydrogenated 1,3-oxazines
    • C07D265/121,3-Oxazines; Hydrogenated 1,3-oxazines condensed with carbocyclic rings or ring systems
    • C07D265/141,3-Oxazines; Hydrogenated 1,3-oxazines condensed with carbocyclic rings or ring systems condensed with one six-membered ring
    • C07D265/181,3-Oxazines; Hydrogenated 1,3-oxazines condensed with carbocyclic rings or ring systems condensed with one six-membered ring with hetero atoms directly attached in position 2
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2601/00Systems containing only non-condensed rings
    • C07C2601/02Systems containing only non-condensed rings with a three-membered ring

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Communicable Diseases (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Virology (AREA)
  • Oncology (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
YU3696A 1995-01-23 1996-01-22 Poboljšana sinteza ciklopropilacetilena YU3696A (sh)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US08/376,611 US5663467A (en) 1995-01-23 1995-01-23 Synthesis of cyclopropylacetylene

Publications (1)

Publication Number Publication Date
YU3696A true YU3696A (sh) 1998-11-05

Family

ID=23485719

Family Applications (1)

Application Number Title Priority Date Filing Date
YU3696A YU3696A (sh) 1995-01-23 1996-01-22 Poboljšana sinteza ciklopropilacetilena

Country Status (23)

Country Link
US (1) US5663467A (cs)
EP (1) EP0805790B1 (cs)
JP (1) JP3107829B2 (cs)
KR (1) KR19980701577A (cs)
CN (1) CN1056824C (cs)
AR (1) AR000771A1 (cs)
AT (1) ATE186903T1 (cs)
AU (1) AU692674B2 (cs)
BR (1) BR9606782A (cs)
CA (1) CA2210577A1 (cs)
CZ (1) CZ234997A3 (cs)
DE (1) DE69605282T2 (cs)
DK (1) DK0805790T3 (cs)
EA (1) EA000074B1 (cs)
ES (1) ES2140062T3 (cs)
FI (1) FI973086L (cs)
GR (1) GR3032200T3 (cs)
HR (1) HRP960029B1 (cs)
HU (1) HUP9800849A3 (cs)
NZ (1) NZ301206A (cs)
SK (1) SK99997A3 (cs)
WO (1) WO1996022955A1 (cs)
YU (1) YU3696A (cs)

Families Citing this family (26)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU3736197A (en) * 1996-07-26 1998-02-20 Du Pont Pharmaceuticals Company A practical synthesis of benzoxazinones useful as hiv reverse transcripta se inhibitors
AU5521498A (en) * 1996-12-16 1998-07-15 Du Pont Pharmaceuticals Company An improved synthesis of cyclopropylacetylene
US5955627A (en) * 1996-12-16 1999-09-21 Kuraray Co., Ltd. Process for the preparation of cyclopropylacetylene derivatives
ZA9711256B (en) 1996-12-16 1999-06-15 Du Pont Merck Pharma Asymmetric synthesis of benzoxazinones
US5932726A (en) * 1996-12-16 1999-08-03 Dupont Pharmaceuticals Company Asymmetric synthesis of benzoxazinones
US5965729A (en) 1997-02-05 1999-10-12 Merck & Co., Inc. Process for the crystallization of a reverse transcriptase inhibitor using an anti-solvent
HU229087B1 (en) * 1997-02-05 2013-07-29 Merck Sharp & Dohme Process for the crystallization of a reverse transcriptase inhibitor using an anti-solvent
US6207864B1 (en) 1997-03-07 2001-03-27 Basf Aktiengesellschaft Process for preparing cyclopropylacetylene
EE9900446A (et) * 1997-04-07 2000-04-17 Dupont Pharmaceuticals Company Bensoksasinoonide asümmeetriline sünteesimine uute vaheühendite kaudu
US6015926A (en) * 1997-05-16 2000-01-18 Merck & Co., Inc. Efficient enantioselective addition reaction using an organozinc reagent
PL338455A1 (en) * 1997-07-31 2000-11-06 Du Pont Pharm Co Metho dof obtaining cyclopropyl acetylene
AU738790B2 (en) * 1997-08-06 2001-09-27 Merck & Co., Inc. Efficient synthesis of cyclopropylacetylene
US6072094A (en) * 1997-08-06 2000-06-06 Merck & Co., Inc. Efficient synthesis of cyclopropylacetylene
ES2170990T3 (es) * 1997-12-10 2002-08-16 Lonza Ag Procedimiento para la preparacion de etinil-ciclopropano.
KR100350752B1 (ko) * 1998-02-06 2002-08-28 가부시키가이샤 구라레 시클로프로필아세틸렌 유도체의 제조방법
US5952537A (en) 1998-03-13 1999-09-14 Wiley Organics, Inc. Preparation of cycloalkylacetylene compounds using dialkylaminomagnesium halide or bis(dialkylamino)magnesium
UA72207C2 (uk) 1998-04-07 2005-02-15 Брістол- Майєрс Сквібб Фарма Компані Фармацевтична композиція ефавіренцу з добавкою дезінтегруючих агентів у вигляді швидкорозчинних капсул або таблеток та спосіб її виготовлення
US20010014352A1 (en) 1998-05-27 2001-08-16 Udit Batra Compressed tablet formulation
US6235957B1 (en) 1998-06-29 2001-05-22 Dupont Pharmaceuticals Company Process for the preparation of cyclopropylacetylene
US6359164B1 (en) 1998-10-01 2002-03-19 Zhe Wang Process for the preparation of cyclopropylacetylene
US6288297B1 (en) 1998-10-01 2001-09-11 Dupont Pharmaceuticals Company Process for the preparation of cyclopropylacetylene
GB2355988A (en) 1999-10-28 2001-05-09 Merck & Co Inc Synthesis of cyclopropylacetylene in a one-pot process using a diazo-keto-phos phonate
GB2355724A (en) * 1999-10-28 2001-05-02 Merck & Co Inc Synthesis of cyclopropylacetylene from propiolic acid (2-propynoic acid)
US8080655B2 (en) * 2009-07-20 2011-12-20 Apotex Pharmachem Inc. Methods of making efavirenz and intermediates thereof
EP2471783A1 (en) 2010-12-23 2012-07-04 Esteve Química, S.A. Novel polymorphic form of efavirenz
CN103254087B (zh) * 2013-06-07 2015-03-18 郑州大学 依非韦伦中间体的制备方法

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SU578293A1 (ru) * 1972-02-04 1977-10-30 Институт Органической Химии Имени Н.Д.Зелинского Ан Ссср Способ получени циклопропилацетилена
SU555079A1 (ru) * 1976-01-30 1977-04-25 Институт органической химии им.Н.Д.Зелинского АН СССР Способ получени циклопропилацетилена
SU572445A1 (ru) * 1976-04-05 1977-09-15 Институт Органической Химии Имени Н.Д. Зелинского Ан Ссср Способ получени циклопропилацетилена

Also Published As

Publication number Publication date
FI973086A7 (fi) 1997-07-22
CA2210577A1 (en) 1996-08-01
DE69605282T2 (de) 2000-07-13
US5663467A (en) 1997-09-02
JPH10512880A (ja) 1998-12-08
KR19980701577A (ko) 1998-05-15
EA000074B1 (ru) 1998-06-25
HRP960029B1 (en) 2000-12-31
EA199700139A1 (ru) 1997-12-30
EP0805790B1 (en) 1999-11-24
AR000771A1 (es) 1997-08-06
CN1056824C (zh) 2000-09-27
ES2140062T3 (es) 2000-02-16
FI973086A0 (fi) 1997-07-22
BR9606782A (pt) 1997-12-30
AU4657496A (en) 1996-08-14
HRP960029A2 (en) 1997-08-31
GR3032200T3 (en) 2000-04-27
AU692674B2 (en) 1998-06-11
CZ234997A3 (cs) 1998-02-18
SK99997A3 (en) 1998-05-06
DE69605282D1 (en) 1999-12-30
HUP9800849A2 (hu) 1999-01-28
FI973086L (fi) 1997-07-22
MX9705562A (es) 1997-10-31
CN1169137A (zh) 1997-12-31
JP3107829B2 (ja) 2000-11-13
EP0805790A1 (en) 1997-11-12
NZ301206A (en) 1998-11-25
ATE186903T1 (de) 1999-12-15
DK0805790T3 (da) 2000-05-01
WO1996022955A1 (en) 1996-08-01
HUP9800849A3 (en) 2001-01-29

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